3-(Pyrrolidin-2-yl)pyridine → HCID 10053082, compound
Reaction equation
CC([O:5][C:6](=[O:42])[C@H:7]([NH:25][C@H:26]([C:31](N(C1CCS(=O)(=O)C1)C)=[O:32])[CH2:27][CH:28]([CH3:30])[CH3:29])[CH2:8][CH2:9][N:10]1[C:18](=[O:19])[C:17]2[CH:16]=[C:15]3[CH:20]=[CH:21][CH:22]=[CH:23][C:14]3=[CH:13][C:12]=2[C:11]1=[O:24])(C)C.[NH:43]1[CH2:47][CH2:46][CH2:45][CH:44]1[C:48]1[CH:49]=[N:50][CH:51]=[CH:52][CH:53]=1>>[O:24]=[C:11]1[C:12]2[CH:13]=[C:14]3[CH:23]=[CH:22][CH:21]=[CH:20][C:15]3=[CH:16][C:17]=2[C:18](=[O:19])[N:10]1[CH2:9][CH2:8][C@@H:7]([NH:25][C@H:26]([C:31]([N:43]1[CH2:47][CH2:46][CH2:45][C@@H:44]1[C:48]1[CH:49]=[N:50][CH:51]=[CH:52][CH:53]=1)=[O:32])[CH2:27][CH:28]([CH3:29])[CH3:30])[C:6]([OH:42])=[O:5]Participants
3
Procedure
Prepared as described in Example 1, Part (a) using 3-pyrrolidin-2-yl-pyridine as HNR2R3 to afford the title compound as a dark solid; 145 mg.
Workup
- customPrepared
Sources & evidence
- ORD record
- ord-7d252dbe81a74484b9fea134d3a28e1b
- Source dataset
- uspto-grants-1994_07
- Patent number
- US05326760
Reaction notes
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